drugset / Trial / NCT02337855

A Phase I Study of the Safety, Reactogenicity, and Immunogenicity of Sm-TSP-2/Alhydrogel® With or Without GLA-AF for Intestinal Schistosomiasis in Healthy Adults

NCT02337855

RandomizedParallel-groupDouble-blindPrevention

Summary

This is a Phase I, first-in-human study of a vaccine against S. mansoni infection.The study will recruit 72 healthy adult males and non-pregnant females from a single clinical center to test two formulations of Sm-TSP-2 vaccine (using the Alhydrogel® only, and using Alhydrogel® plus GLA-AF), each at 3 different doses: 10ug, 30ug, and 100ug. The primary objective is to assess the safety and reactogenicity of ascending doses of Sm-TSP-2/Alhydrogel® (10ug, 30ug, or 100ug) with or without GLA-AF vaccine given as three doses administered on Days 1, 57, and 113.

Timeline

Start
2015-02-04
Primary completion
2017-01-27
Completion
2017-01-27

Drugs

EvaluationDrugModalityDoseRoute
Subject GLA-AF Other / unclassified Intramuscular
Subject Sm-TSP-2 Vaccine 10 ug Intramuscular
Subject Sm-TSP-2 Vaccine 30 ug Intramuscular
Subject Sm-TSP-2 Vaccine 100 ug Intramuscular
Background Aluminum hydroxide Unknown Intramuscular